ClinGen Allele Registry
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Canonical Allele Identifier:
CA196389180
Gene:
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chr9:g.93868852A>T
GRCh37
chr9:g.96631134A>T
Linked Data - Sequence & Population
gnomAD v2:
9:96631134 A / T
gnomAD v3:
9:93868852 A / T
gnomAD v4:
chr9-93868852-A-T
Joint Max Group AF
0.36538485 (NFE)
Genomes Max Group AF
0.36538485 (NFE)
Linked Data - NCBI & NCI
dbSNP:
10114408
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000009.12:g.93868852A>T , CM000671.2:g.93868852A>T
GRCh38
NC_000009.11:g.96631134A>T , CM000671.1:g.96631134A>T
GRCh37
NC_000009.10:g.95670955A>T
NCBI36
Search 100 bp 5'
Search 100 bp 3'